OK2STANDUP INC.

FDA Device Registration & Listing · Bedford, PA, US · Registration 3032856309

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3032856309
FEI Number
3032856309
Entity Name
OK2STANDUP INC.
City/State/Country
Bedford, PA, US
Establishment Address
1 Corporate Dr Ste 101, Bedford, PA 15522, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
OK2StandUP Inc. (Owner Number: 10091455)
Owner / Operator Contact Address
1 Corporate Dr, Suite 101, Bedford, PA 15522, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

OK2StandUP System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PJO Fall Prevention Alarm/Sensor Combination Attached Or Unattached General Hospital Class 1 880.2400 2024-10-04

Official Correspondent

Eunice Yang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OK2StandUP Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032856309. Last updated year: 2026. Please use registration number 3032856309 when referencing this establishment in official correspondence.
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